Canonical Allele Identifier: PA2499235927
Gene: RPGR HGNC NCBI

Linked Data

ClinVar Variation Id: 1012373
ClinVar RCV Id: RCV001310291
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001030025.1:p.Trp1141Cys
CA412726237
NM_001034853.2:c.3423G>T
CA412726240
NM_001034853.2:c.3423G>C